Canonical Allele Identifier: CA2619452956
Gene: INHBC HGNC NCBI

Linked Data

gnomAD v4: 12-57450271-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57450271G>A , CM000674.2:g.57450271G>A GRCh38
NC_000012.11:g.57844054G>A , CM000674.1:g.57844054G>A GRCh37
NC_000012.10:g.56130321G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309668.3:c.*249G>A MANE Select ENSP00000308716.2:n.*249G>A
ENST00000309668.2:c.*249G>A ENSP00000308716.2:n.*249G>A
NM_005538.3:c.*249G>A NP_005529.1:n.*249G>A
NM_005538.4:c.*249G>A MANE Select NP_005529.1:n.*249G>A
Search 100 bp 5'
Search 100 bp 3'